Decarbonylation Colchicine: Properties, Uses & FAQs
Decarbonylation Colchicine: Properties, Uses & FAQs
Decarbonylation colchicine is a structural analog of colchicine in which the C-10 carbonyl group has been removed, resulting in a compound used in research to probe the structure–activity relationships of the colchicine binding site on tubulin.
- Product Name
- Decarbonylation colchicine
- SKU / Catalog Number
- D768317
- Compound Class
- Colchicine structural analog; antimitotic alkaloid derivative
- Primary Research Use
- Tubulin binding site characterization; structure–activity relationship (SAR) studies
- Key Structural Feature
- Carbonyl group at C-10 position of the tropolone ring is absent compared to parent colchicine
- Storage Recommendation
- Store at −20 °C, protected from light and moisture (verify with product datasheet)
What Is Decarbonylation Colchicine?
Decarbonylation colchicine is a synthetic analog of the natural alkaloid colchicine, differing by the removal of the carbonyl (C=O) group from the tropolone C-ring. Colchicine itself is a well-characterized inhibitor of tubulin polymerization, binding at the colchicine site on β-tubulin and preventing microtubule assembly. The decarbonylated derivative is used in research contexts primarily to investigate how this carbonyl moiety contributes to binding affinity, selectivity, and biological potency at the colchicine binding site.
As a research reagent (Aladdin SKU D768317), Decarbonylation colchicine provides scientists with a tool to conduct structure–activity relationship (SAR) studies, helping to define the pharmacophoric requirements of colchicine-site ligands without the full pharmacological profile of the parent compound.
Structural Comparison with Colchicine
Colchicine is composed of three rings: a trimethoxyphenyl A-ring, a seven-membered B-ring bearing an acetamido group, and a tropolone C-ring containing a carbonyl and a methoxy substituent. Decarbonylation colchicine retains the A- and B-ring framework but lacks the carbonyl functionality on the C-ring.
This structural simplification is scientifically significant: the carbonyl group of colchicine's tropolone ring participates in key interactions with residues in the colchicine binding pocket of tubulin. Removal of this group is therefore expected to modulate (typically reduce) binding affinity, making the compound a valuable negative-control or SAR probe in comparative tubulin-binding assays.
Note: Specific binding affinity data (Kd values) for Decarbonylation colchicine versus colchicine should be verified against primary literature; no specific figures are provided in the current product documentation.
Research Applications and Handling
Research Applications: Decarbonylation colchicine is primarily employed in:
- Structure–activity relationship (SAR) studies at the colchicine binding site of tubulin
- Comparative binding assays (e.g., competitive displacement assays using fluorescent colchicine analogs)
- Mechanistic investigation of tubulin–ligand interactions
- Serving as a reference compound in antimitotic drug discovery programs
Solubility and Formulation: Like colchicine, this analog is expected to be soluble in common organic solvents such as DMSO and ethanol. Aqueous solubility may be limited. Researchers should prepare stock solutions in DMSO and dilute into aqueous buffers or cell culture media immediately before use. Final DMSO concentration in biological assays should be kept ≤0.1% to minimize solvent effects. (Verify solubility data against the product Certificate of Analysis.)
Safety: Colchicine and its analogs are toxic compounds. Although Decarbonylation colchicine may have altered pharmacological activity relative to colchicine, it should be handled with appropriate caution: use gloves, work in a well-ventilated area or fume hood, and consult the Safety Data Sheet (SDS) before use.
Storage, Stability, and Quality
Recommended Storage: Store Decarbonylation colchicine at −20 °C in a tightly sealed container, protected from light and moisture. As with most alkaloid derivatives, repeated freeze–thaw cycles should be avoided to preserve compound integrity.
Stability: The compound is expected to be stable under the recommended storage conditions for an extended period; however, researchers should verify the expiry date and lot-specific stability data provided on the Certificate of Analysis (CoA) supplied with each order.
Purity and Quality: Aladdin Scientific reagents are quality-controlled prior to release. The purity specification and analytical data (e.g., HPLC, NMR, MS) for SKU D768317 are available on the product CoA. Researchers requiring high-purity material for quantitative binding studies should confirm purity ≥95% on the CoA before use.
Note: The source description references a related product at McLean (麦克林) catalog number D885897. Researchers should confirm they are ordering the correct product from Aladdin (D768317) and cross-reference specifications as needed.
Ordering and Support
How to Order: Decarbonylation colchicine (SKU D768317) is available from Aladdin Scientific. To place an order, visit the Aladdin Scientific website, search by SKU D768317 or product name, and add to cart. For bulk quantities or custom requirements, contact the Aladdin sales team directly.
Technical Support: For technical questions about this product—including solubility, formulation recommendations, or application-specific guidance—please contact Aladdin Scientific's technical support team via the website or by email. Our specialists can assist with protocol development and reagent selection.
Documentation: The Safety Data Sheet (SDS) and Certificate of Analysis (CoA) for each lot are available for download from the product page or upon request from customer service.
Frequently asked questions
What is the difference between Decarbonylation colchicine and colchicine?
Decarbonylation colchicine is a structural analog of colchicine from which the carbonyl group on the tropolone C-ring has been removed. This modification alters its interaction with the colchicine binding site on β-tubulin, typically reducing binding affinity compared to the parent compound. It is used as a research probe rather than as a replacement for colchicine.
What solvents can be used to dissolve Decarbonylation colchicine?
Decarbonylation colchicine is expected to be soluble in organic solvents such as DMSO and ethanol, consistent with the physicochemical properties of colchicine analogs. Aqueous solubility may be limited. Stock solutions should be prepared in DMSO and diluted into the desired aqueous medium immediately before use. Always verify solubility data on the product Certificate of Analysis (CoA).
What are the recommended storage conditions for Decarbonylation colchicine (D768317)?
The compound should be stored at −20 °C in a tightly sealed container, away from light and moisture. Avoid repeated freeze–thaw cycles. Always refer to the lot-specific Certificate of Analysis for confirmed storage conditions and expiry date.
Is Decarbonylation colchicine suitable for cell-based assays?
Decarbonylation colchicine may be used in cell-based research assays as a comparative or control compound alongside colchicine in studies of tubulin dynamics. Because its tubulin-binding activity is expected to differ from colchicine due to the absent carbonyl, researchers should titrate concentrations carefully and validate activity in their specific assay system. Keep DMSO vehicle concentration ≤0.1% in culture media.
How does Aladdin's Decarbonylation colchicine (D768317) relate to the McLean catalog number D885897?
The product description notes a cross-reference to McLean (麦克林) catalog number D885897, suggesting a related or equivalent listing. Researchers sourcing from Aladdin Scientific should use SKU D768317 and confirm specifications via the Aladdin product page and Certificate of Analysis to ensure the material meets their requirements.
References
- Hastie SB. Interactions of colchicine with tubulin. Pharmacol Ther. 1991;51(3):377-401. [General reference on colchicine-tubulin binding; specific data for decarbonylation analog not confirmed in source material.]
- Bhattacharyya B, Panda D, Gupta S, Banerjee M. Anti-mitotic activity of colchicine and the structural basis for its interaction with tubulin. Med Res Rev. 2008;28(1):155-183. [General reference; applicability to decarbonylation analog needs verification.]
Products are supplied for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
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